WO2004006919A1 - 血中脂質改善又は血中ホモシステイン低下のための医薬組成物 - Google Patents
血中脂質改善又は血中ホモシステイン低下のための医薬組成物 Download PDFInfo
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- WO2004006919A1 WO2004006919A1 PCT/JP2003/008674 JP0308674W WO2004006919A1 WO 2004006919 A1 WO2004006919 A1 WO 2004006919A1 JP 0308674 W JP0308674 W JP 0308674W WO 2004006919 A1 WO2004006919 A1 WO 2004006919A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
- A61K31/675—Phosphorus compounds having nitrogen as a ring hetero atom, e.g. pyridoxal phosphate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4415—Pyridoxine, i.e. Vitamin B6
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Definitions
- the present invention relates to a pharmaceutical composition (particularly, a pharmaceutical composition for improving blood lipids or high blood homocystin) containing an HMG-CoA reductase inhibitor and pyridoxines.
- Homocysteine is an amino acid that is produced during the metabolism of methionine, one of the essential amino acids, but has a genetic predisposition, lack of vitamin cofactors (folate, vitamin B6, vitamin B12), aging, sex, and kidney. It has been shown that the amount of homocysteine in blood increases due to functional decline, diabetes, other diseases, drugs, smoking, etc. (Progress in Medicine, Vol.19 No.8, 1999 p.49-52), This condition is called hyperhomocysteinemia. At present, folate administration to facilitate homocystin metabolism is the first step treatment for hyperhomocysteinemia, and vitamin B6 and vitamin B12 are administered as the second step ( Progress in Medicine, Vol.19 No.8, 1999 p.52-53).
- statins are drugs that specifically and competitively inhibit HMG-CoA reductase in the living body to lower the blood cholesterol level.
- statins and pyridoxines are described in WO 97Z38694, page 17, in addition to statins and folic acid, HMG-CoA synthetase inhibitor, squalene epoxidase inhibitor, squalene Synthetase inhibitor, ACAT inhibitor, Probucol, Niacin, Fibrate, Cholesterol absorption inhibitor, Bile acid adsorbent, LDL receptor inducer, Vitamin B 6, Vitamin B 12, Aspirin, Better blocker, Vitamin C, Vitamin And that selected from E and beta-carotene.
- WO 97/38694 does not describe the combination use of the HMG-CoA synthetase inhibitor of the present invention and a pyridoxine, and the effect of the present invention, that is, the remarkable improvement of the blood lipid of the present invention. There is no description or suggestion of any action or the manifestation of a markedly lowering action of the blood homocysteine level.
- WO 02/43659 also states that HMG-CoA reductase inhibitor (statin) and 7 kinds of sub-fragments ( ⁇ -3 fatty acids, Vitamin II, vitamin C, vitamin B6, vitamin B12, folic acid, calcium) are disclosed.
- statins and ⁇ -3 fatty acids improve serum lipids
- vitamins ⁇ and C have antioxidant effects
- the combination of folic acid and vitamins ⁇ 6 and B12 Decreases homocystin levels
- calcium reduces blood pressure in the heart It is a composition devised based on the presumption that it is useful for vascular health, and no specific test data has been disclosed.Therefore, the present invention has been disclosed in WO 02/43659. There is no description or suggestion about the effect, that is, the expression of the remarkable improving effect of blood lipid and the remarkable lowering effect of blood homocystin level of the present invention.
- the present inventors have conducted intensive studies to find a safe drug that improves blood lipids and a safe drug that lowers the amount of homocysteine in the blood. As a result, HMG-CoA reductase inhibitor and pyridoxine The present inventors have found that a remarkable blood lipid improving effect and a blood homocystin level lowering effect are exhibited when used in combination with, and the present invention has been completed.
- a pharmaceutical composition comprising a HMG-CoA reductase inhibitor and a pyridoxine.
- the pharmaceutical composition is
- composition according to (1) for improving blood lipid or high homocysteine in blood
- HMG-CoA reductase inhibitors selected from the group consisting of pravastatin, oral bacterin, simpastatin, flupastatin, rivastatin, atorvastatin, pistapastin and rosuvastin Or two or more,
- composition according to (1) or (2) The composition according to (1) or (2),
- the HMG-CoA reductase inhibitor is one or more selected from the group consisting of pravastatin, simvastatin or atorpastatin, (1) or
- the pyridoxine is one or more selected from the group consisting of pyridoxine, pyridoxal, pyridoxamine or a salt thereof; (1) to (5) A composition according to any one of the selected,
- composition according to (2) wherein the HMG-CoA reductase inhibitor is atorvastatin or a salt thereof, and the pyridoxine is pyridoxine or a salt thereof.
- composition according to any one of (1) to (8), for improving a high homocysteine level in blood (10) The composition according to any one of (1) to (8), for improving a high homocysteine level in blood,
- Hyperlipidemia arteriosclerosis, ischemic heart disease, myocardial infarction, thrombosis, peripheral vascular disease, Burger disease, Raynaud disease, cerebral infarction, cerebral circulatory insufficiency, senile dementia, Alzheimer's disease or Parkinson's disease
- HMG-Co for improving the blood lipid or high homocysteine level in the blood by simultaneously or separately administering the HMG-CoA reductase inhibitor and the pyridoxine.
- HMG-CoA reductase inhibition for producing a pharmaceutical composition for improving blood lipids or lowering blood homocystin, comprising an HMG-CoA reductase inhibitor and a pyridoxine Of drugs and pyridoxine
- HMG-CoA reductase inhibitor which is one of the components of the pharmaceutical composition of the present invention Is a drug that specifically and competitively inhibits HMG (3-hydroxy-13-methylidalaryl) -CoA reductase, the rate-limiting enzyme in the cholesterol biosynthesis system. Because it lowers blood cholesterol, it is originally used as a therapeutic agent for hyperlipidemia.
- HMG-CoA reductase inhibitors include all natural substances derived from microorganisms, semi-synthetic substances derived therefrom, and all synthetic compounds. For example, Japanese Patent Publication No. US Pat. No.
- HMG—CoA reducer Such as isopropyl-2- (N-methyl-1-N-methanesulfonylamino) pyrimidine-1-5- ⁇ ⁇ ]]-3,5-dihydroxy-16 (E) -monoheptenic acid (hereinafter abbreviated as rospastatin) HMG—CoA reducer, which is a component of the pharmaceutical composition of the present invention.
- Hose inhibitors also include other HMG—CoA reductase inhibitors disclosed in the publications describing the above HMG—CoA reductase inhibitors.
- Rosbas quintin Pyridoxine which is one of the components of the pharmaceutical composition of the present invention, refers to pyridoxine, pyridoxal, pyridoxamine or a salt thereof, and preferably, pyridoxine hydrochloride, pyridoxal phosphate Or pyridoxamine phosphate, and more preferably pyridoxine hydrochloride.
- each of the above-mentioned components may be contained as a pharmacologically acceptable salt.
- hydrohalides such as hydrofluoride, hydrochloride, hydrobromide, hydroiodide; nitrate, perchlorate, sulfuric acid Salts, inorganic salts such as phosphates; lower organic sulfonates such as methanesulfonate, trifluoromethanesulfonate, and ethanesulfonate; benzenesulfonate, P-to Arylsulfonates such as ruenesulfonate; amino acid salts such as ordinate and glutamate; and carboxyls such as fumaric acid, succinic acid, cunic acid, tartaric acid, oxalic acid and maleic acid. Acid salts,
- the component may be an alkaline metal salt such as a sodium, potassium, or lithium salt, an alkaline earth metal salt such as a calcium or magnesium salt, an aluminum salt, an iron salt, Metal salts such as zinc salts, copper salts, nickel salts, and cobalt salts; inorganic salts such as ammonium salts, t-octylamine salts, dibenzylamine salts, morpholine salts, dalcosamine salts, phenylglycine alkyl ester salts, and ethylenediamine salts.
- alkaline metal salt such as a sodium, potassium, or lithium salt
- an alkaline earth metal salt such as a calcium or magnesium salt, an aluminum salt, an iron salt
- Metal salts such as zinc salts, copper salts, nickel salts, and cobalt salts
- inorganic salts such as ammonium salts, t-octylamine salts, dibenzylamine salts, morpholine salts,
- N-methyldalcamine salt, guanidine salt getylamine salt, triethylamine salt, dicyclohexylamine salt, N, N'-dibenzylethylenediamine salt, black mouth pro-force salt, pro-force salt, jetano Lamine salts, N-benzyl-phenethylamine salts, piperazine salts, tetramethylammonium salts, Amine salts such as organic salts such as tris (hydroxymethyl) aminomethane salt may be mentioned, for example, in the case of brapastatin, preferably sodium pravastatin, for example, in the case of atorpastatin, preferably atorvastatin It is calcium hydrate.
- a pharmaceutical composition containing the hydrate or solvate is also included in the present invention.
- "improving blood lipids” means lowering blood lipids to a clinically significant degree, that is, lowering blood triglycerides, lowering blood LDL, or It means lowering total blood cholesterol.
- “improving a high blood homocysteine level” means suppressing an increase in the blood high homocysteine level and reducing the blood high homocysteine level.
- the term "disease caused by high blood homocystin level” refers to blood homocystin.
- circulation such as arteriosclerosis, ischemic heart disease, myocardial infarction, thrombosis, peripheral vascular disorder, Burger disease, Raynaud disease, etc.
- cerebrovascular disorders such as cerebral infarction, cerebral insufficiency, senile dementia, and nervous system diseases such as Alzheimer's disease and Parkinson's disease.
- the subjective symptoms related to the “disease caused by high blood homocystin level” in the present invention include, for example, headache, Headache, dizziness, numbness or numbness, cold limbs, stiff shoulders. Therefore, the above-mentioned diseases can be treated at an early stage by using the pharmaceutical composition of the present invention for these subjective symptoms.
- the HMG-CoA reductase inhibitor contained in the pharmaceutical composition of the present invention for example, pravastin, oral baths, simpastatin, flubassin, rivastinstin, atorvastatin, pitavastin, or rossavusin JP-A-57-2240 (USP4346227), JP-A-57-163374 (USP4231938), JP-A-56-122375 (USP4444784), Tokushusho 60 — 5000 15 Publication (US P473907 3), JP-A 1-216974 (US P 5006 530), JP-A 3-58967 (US P 5273995), JP 1-279866 ( It can be easily produced according to the method described in US Pat. No. 5,854,259 and US Pat. No. 5,856,336) or JP-A-5-178841 (US Pat. No. 5,260,440).
- a commercially available pyridoxine can be obtained, or a pyridoxine produced by a known method can be used. It is listed in the Japanese Pharmacopoeia and can be easily obtained.
- the “pharmaceutical composition containing an HMG-CoA reductase inhibitor and a pyridoxine” of the present invention comprises an essential component comprising an HMG-CoA reductase inhibitor and a pyridoxine. It may be contained as an ingredient and, if desired, may contain additives for formulation.Furthermore, as long as it does not adversely affect the combined action of the HMG-CoA reductase inhibitor and pyridoxine. Other components may be contained. Preferably, it is a pharmaceutical composition containing only the ⁇ 110-80-reductase inhibitor and pyridoxine as active ingredients, and further containing additives for formulation.
- Specific dosage forms of the pharmaceutical composition of the present invention include, for example, tablets, fine granules (including powders), capsules, liquids (including syrups), and the like. It can be produced according to a usual method described in the Japanese Pharmacopoeia or the like, using additives and base materials as appropriate.
- lactose or purified sucrose is used as an excipient
- metasilicate, magnesium aluminate or magnesium oxide is used as a stabilizer
- corn starch is used as an adsorbent
- hydroxypropyl cellulose is used as a binder As can be used.
- a disintegrating agent such as crospovidone; a surfactant such as polysorbate; an adsorbent such as calcium silicate; a coloring agent such as iron sesquioxide and caramel; a stabilizer such as sodium benzoate; PH regulators, fragrances, etc.
- a disintegrating agent such as crospovidone
- a surfactant such as polysorbate
- an adsorbent such as calcium silicate
- a coloring agent such as iron sesquioxide and caramel
- a stabilizer such as sodium benzoate
- each component can be administered simultaneously or separately at an interval.
- the “simultaneous” administration described above includes administration at exactly the same time as well as administration at about the same time as pharmacologically permitted.
- the dosage form is almost There is no particular limitation as long as the dosage form can be administered at the same time, but a single composition is preferred.
- the above-mentioned “separately administered at different times” is not particularly limited as long as it can be administered separately at different times, but for example, one component is administered, and then After a period of time, other components may be administered.
- ⁇ administering simultaneously or separately at intervals '' refers to the method of administering all of them at the same time. And two or more drugs are administered simultaneously and the remaining drugs are administered at a later time, or two or more drugs are administered at a later time and the remaining drugs are administered simultaneously.
- the pharmaceutical composition of the present invention has a remarkable blood lipid improving effect and a blood homocysteine lowering effect, it can be used as a drug for improving blood lipid or blood high homocysteine, For example, prevent hyperlipidemia, arteriosclerosis, ischemic heart disease, myocardial infarction, thrombosis, peripheral vascular disease, Burger disease, Raynaud disease, cerebral infarction, cerebral circulatory insufficiency, senile dementia, Alzheimer's disease or Parkinson's disease Alternatively, it can be used as a therapeutic drug.
- the dose of the HMG-CoA reductase inhibitor varies depending on the type, dosage form, etc. of the HMG-CoA reductase inhibitor, but is usually 1 mg to 20 Omg per day, preferably 5 mg to 16 Omg per day.
- the dose of pyridoxine varies depending on the type, dosage form, etc. of the pyridoxine, but is usually 0.1 mg to 120 mg per day, preferably 1 mg to 80 mg per day. It is.
- the weight% of the component contained is, for example, usually 0.01 to 5% in the case of atorpastatin and bra. Pastatin, and preferably 0 to 5%.
- 0.05 to 3% and in the case of simpastatin, it is usually 0.05 to 3%, preferably 0.03 to 2%, and the weight% of pyridoxine is Usually 0.01 to 30%, preferably 0.1 to 20% It is.
- the amount of the components contained is, for example, the content of atlubasitin and pravastin is usually 0.01 to 1 O mg / mL. Is 0.05 to 5 mg / mL, and the content of simvastatin is usually 0.05 to 5 mg / mL, preferably 0.3 to 3 mg / mL.
- the pyridoxine content is usually 0.1 to 20 mg / mL, preferably 1 to 10 mg / mL.
- 6 cuffs 6 cuffs. 6 cuffs in the cell. 6 cuffs in the cell. In the cell
- Puravasuchinnatorium was manufactured by Sankyo Co., Ltd.
- Simpastatin and atorvastatin calcium were manufactured by Chemtech Lab Co., Ltd.
- pyridoxine hydrochloride was manufactured by Nippon Roche Co., Ltd.
- beagle dogs and males were purchased from Covance Research Products Inc. at the age of 5 months and used after quarantine and acclimatization for about 1 month.
- test substance calculated based on the body weight of each test animal was filled into a TORPAC gelatin capsule (12 oz). After filling, capsules are sorted by animal type. And stored refrigerated until administration.
- the capsules filled with the test substance were administered by oral gavage to the test animals once a day between 9:00 and 12:30.
- the test animals were fasted for 2 to 3 hours before administration.
- the administration period was 11 days.
- the obtained blood was placed in a test tube, allowed to stand at room temperature for 30 minutes to 1 hour, and then centrifuged (about 1,600 Xg, 10 minutes), and the serum obtained was used.
- test results were as follows: total cholesterol was measured by an enzymatic method, HDL was measured by a homogenous method, LDL was measured by a chemically modified enzyme method, and triglyceride was measured by a whole enzyme method.
- An automatic clinical chemistry analyzer TAA-120FR, manufactured by Toshiba was used for the measurement.
- Tables 1 to 6 show the obtained results. Each value is the average of 5 animals per group. Table 1
- Vitrabasin calcium was manufactured by Chemtech Lab Co., Ltd., and pyridoxine hydrochloride was manufactured by Roche Japan.
- beagle dogs and males were purchased from Covance Research Products Inc. at the age of 5 months and used after quarantine and acclimatization for about 1 month.
- the required amount of the test substance calculated based on the body weight of each test animal was filled into a T0RPAC gelatin capsule (1 oz.). After filling, the capsules were placed in cases classified for each animal and kept refrigerated until administration.
- the capsule filled with the test substance was administered by oral gavage to the test animal once a day between 9:00 and 12:30.
- the test animals were fasted for 2 to 3 hours before administration.
- the administration period was 11 days.
- the obtained blood was placed in a test tube, allowed to stand at room temperature for 30 minutes to 1 hour, and then centrifuged (about 1,600 X g, 10 minutes), and the obtained serum was used.
- the blood homocysteine level was determined using the HPLC method commonly used in clinical tests.
- the blood homocysteine amount of each of atorvastatin calcium and pyridoxine hydrochloride alone and in combination was calculated as the average of the blood homocystin levels two weeks before and one week before administration, which was 100. I asked.
- Table 7 shows the obtained results. Each value is the average of 5 animals per group.
- composition containing the HMG-CoA reductase inhibitor of the present invention and pyridoxine Since the product has an excellent blood lipid improving effect and blood homocysteine lowering effect, hyperlipidemia, arteriosclerosis, ischemic heart disease, myocardial infarction, thrombosis, peripheral vascular disorder, Burger disease, Raynaud disease It is useful for preventing or treating cardiovascular diseases such as cerebral infarction, cerebral circulatory insufficiency, senile dementia and other nervous system diseases such as Alzheimer's disease and Parkinson's disease.
- blood homogen caused by aging, smoking, nutritional disorders related to homocystin metabolism, drug-induced, decreased renal function, chronic renal failure, diabetes, insulin resistance, malignant tumor, hypothyroidism, pernicious anemia, etc. It is useful for preventing or treating an increase in the amount of cysteine.
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Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA002492781A CA2492781A1 (en) | 2002-07-11 | 2003-07-08 | Medicinal composition for mitigating blood lipid or lowering blood homocystein |
AU2003281176A AU2003281176A1 (en) | 2002-07-11 | 2003-07-08 | Medicinal composition for mitigating blood lipid or lowering blood homocystein |
US11/031,105 US20050182106A1 (en) | 2002-07-11 | 2005-01-07 | Medicinal composition for mitigating blood lipid or lowering blood homocysteine |
HK05111986A HK1077232A1 (en) | 2002-07-11 | 2005-12-23 | Medicinal composition for mitigating blood lipid or lowering blood homocystein |
US11/980,937 US20080070938A1 (en) | 2002-07-11 | 2007-10-31 | Medicinal composition for mitigating blood lipid or lowering blood homocysteine |
Applications Claiming Priority (4)
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JP2002202121 | 2002-07-11 | ||
JP2002-202121 | 2002-07-11 | ||
JP2002343586 | 2002-11-27 | ||
JP2002-343586 | 2002-11-27 |
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US11/031,105 Continuation-In-Part US20050182106A1 (en) | 2002-07-11 | 2005-01-07 | Medicinal composition for mitigating blood lipid or lowering blood homocysteine |
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WO2004006919A1 true WO2004006919A1 (ja) | 2004-01-22 |
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JP (1) | JP2010077162A (ja) |
CN (1) | CN100341509C (ja) |
AU (1) | AU2003281176A1 (ja) |
CA (1) | CA2492781A1 (ja) |
HK (1) | HK1077232A1 (ja) |
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Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005060975A1 (en) * | 2003-12-23 | 2005-07-07 | Medicure International Inc. | Combination therapies employing a composition comprising a hmg coa reductase inhibitor and a vitamin b6 related compound |
WO2006033287A1 (ja) * | 2004-09-21 | 2006-03-30 | Sankyo Company, Limited | HMG-CoAリダクターゼ阻害剤とグルタチオンを含有する医薬組成物。 |
JP2006117645A (ja) * | 2004-09-21 | 2006-05-11 | Sankyo Co Ltd | HMG−CoAリダクターゼ阻害剤とグルタチオンを含有する医薬組成物 |
US9597289B2 (en) * | 2006-04-26 | 2017-03-21 | Rosemont Pharmaceuticals Ltd. | Liquid oral simvastatin compositions |
WO2020046132A1 (en) | 2018-08-31 | 2020-03-05 | Leiden University | Pharmacological chaperones for enzyme treatment therapy |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2015060317A1 (ja) * | 2013-10-22 | 2015-04-30 | 長谷川亨 | 神経変性疾患の検査方法 |
JP6009050B1 (ja) * | 2015-08-21 | 2016-10-19 | 国立大学法人東北大学 | 飲酒による悪酔いまたは二日酔いの軽減または予防剤 |
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EP0595005A1 (en) * | 1992-09-14 | 1994-05-04 | Vesta Medicines (Proprietary) Limited | Pharmaceutical preparations for lowering homocysteine levels, containing vitamin B6, folic acid and vitamin B12 |
WO1997038694A1 (en) * | 1996-04-17 | 1997-10-23 | Merck & Co., Inc. | Combination therapy for reducing the risks associated with cardiovascular disease |
WO1999020110A1 (en) * | 1997-10-22 | 1999-04-29 | Merck & Co., Inc. | Combination therapy for reducing the risks associated with cardio- and cerebrovascular disease |
WO2001003696A1 (en) * | 1999-07-14 | 2001-01-18 | Laxdale Limited | Pharmaceutical and nutritional compositions containing essential fatty acids and homocysteine-lowering agents |
WO2002043659A2 (en) * | 2000-11-29 | 2002-06-06 | Smithkline Beecham Corporation | Composition containing statins and calcium for improved cardiovascular health |
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US6669955B2 (en) * | 2001-08-28 | 2003-12-30 | Longwood Pharmaceutical Research, Inc. | Combination dosage form containing individual dosage units of a cholesterol-lowering agent, an inhibitor of the renin-angiotensin system, and aspirin |
-
2003
- 2003-07-08 WO PCT/JP2003/008674 patent/WO2004006919A1/ja active Application Filing
- 2003-07-08 CA CA002492781A patent/CA2492781A1/en not_active Abandoned
- 2003-07-08 AU AU2003281176A patent/AU2003281176A1/en not_active Abandoned
- 2003-07-08 CN CNB038216418A patent/CN100341509C/zh not_active Expired - Fee Related
- 2003-07-10 TW TW092118805A patent/TWI302457B/zh not_active IP Right Cessation
-
2005
- 2005-12-23 HK HK05111986A patent/HK1077232A1/xx not_active IP Right Cessation
-
2010
- 2010-01-08 JP JP2010002651A patent/JP2010077162A/ja active Pending
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EP0595005A1 (en) * | 1992-09-14 | 1994-05-04 | Vesta Medicines (Proprietary) Limited | Pharmaceutical preparations for lowering homocysteine levels, containing vitamin B6, folic acid and vitamin B12 |
WO1997038694A1 (en) * | 1996-04-17 | 1997-10-23 | Merck & Co., Inc. | Combination therapy for reducing the risks associated with cardiovascular disease |
WO1999020110A1 (en) * | 1997-10-22 | 1999-04-29 | Merck & Co., Inc. | Combination therapy for reducing the risks associated with cardio- and cerebrovascular disease |
WO2001003696A1 (en) * | 1999-07-14 | 2001-01-18 | Laxdale Limited | Pharmaceutical and nutritional compositions containing essential fatty acids and homocysteine-lowering agents |
WO2002043659A2 (en) * | 2000-11-29 | 2002-06-06 | Smithkline Beecham Corporation | Composition containing statins and calcium for improved cardiovascular health |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2005060975A1 (en) * | 2003-12-23 | 2005-07-07 | Medicure International Inc. | Combination therapies employing a composition comprising a hmg coa reductase inhibitor and a vitamin b6 related compound |
WO2006033287A1 (ja) * | 2004-09-21 | 2006-03-30 | Sankyo Company, Limited | HMG-CoAリダクターゼ阻害剤とグルタチオンを含有する医薬組成物。 |
JP2006117645A (ja) * | 2004-09-21 | 2006-05-11 | Sankyo Co Ltd | HMG−CoAリダクターゼ阻害剤とグルタチオンを含有する医薬組成物 |
US9597289B2 (en) * | 2006-04-26 | 2017-03-21 | Rosemont Pharmaceuticals Ltd. | Liquid oral simvastatin compositions |
US10300041B2 (en) | 2006-04-26 | 2019-05-28 | Rosemont Pharmaceuticals Ltd | Liquid oral simvastatin compositions |
WO2020046132A1 (en) | 2018-08-31 | 2020-03-05 | Leiden University | Pharmacological chaperones for enzyme treatment therapy |
Also Published As
Publication number | Publication date |
---|---|
HK1077232A1 (en) | 2006-02-10 |
AU2003281176A1 (en) | 2004-02-02 |
CN100341509C (zh) | 2007-10-10 |
CN1681499A (zh) | 2005-10-12 |
CA2492781A1 (en) | 2004-01-22 |
TWI302457B (en) | 2008-11-01 |
JP2010077162A (ja) | 2010-04-08 |
TW200403053A (en) | 2004-03-01 |
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